Terumo Cardiovascular Systems Corporation

데이터베이스에서 발견된 의료기기 1건 데이터베이스에서 발견된 의료기기 12 건

  • 모델명 / 제조번호(시리얼번호)
    6912 , 6913 6914, 6932, 6933 6934, 6922, 6923 6924, CV-6912, CV-6913, CV-6914 Cardiovascular Procedure Kits- Various
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide Distribution - USA (nationwide) Distribution.
  • 제품 설명
    CDI¿ H/S Cuvette || The intended use for the CDI¿ H IS Cuvette is as follows: The CDI¿ H/S Cuvettes are intended for use with a CDI monitor during cardiopulmonary bypass procedures when continuous monitoring of blood hematocrit and oxygen saturation is desired.
  • 모델명 / 제조번호(시리얼번호)
    Serial Number Range 70194 through 70504
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    Terumo Cardiovascular has identified 16 domestic consignees and 30 international consignees .
  • 제품 설명
    Hercules 360 Universal Stabilizing Arm, top mount, 360-degree rotation, reusable stainless steel
  • 모델명 / 제조번호(시리얼번호)
    Catalog Number: 401-231, Product Description: Titan" Stabilizer Attachment , Lot Number: 052R   Catalog Number 401-231u , Product Description TitanTM 360 Stabilizer Attachment , Lot Number: 020R, 024R, 026R, 029R, 030R,034R,035R,037R, 040 , 048R
  • 의료기기 분류등급
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    The product was distributed domestically and also to foreign consignees. But not to government agency's or Canada.
  • 제품 설명
    Titan" Stabilizer Attachment and Titan TM 360 Stabilizer || Attachment
  • 모델명 / 제조번호(시리얼번호)
    TAOS, TC03
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Terumo CVS has identified 33 domestic consignees and 0 international consignee that are affected by this recall
  • 제품 설명
    The Sarns Centrifugal Pump is a single use device sterilized by ethylene oxide gas. The device is sold single sterile in cartons of 8 units, or may be provided in bulk, non-sterile to another Terumo location for inclusion in Cardiovascular Procedure Kits. Cardiovascular Procedure kits are packaged individually.
  • 모델명 / 제조번호(시리얼번호)
    SAFETY ALERT Lot Codes:  (a) RH14, RK11, RK20, RL02, RM06, RM20, RN10, RP08, TD16, TE13, TE27, TF14, TF21, TG04, TG11, TG17, TH06, TH16, TK10, TK24, TL08, TL21, TM28, TP14, UA11, UA18, UA25, UC08, UC22, UD14, UD21, UD28, UE05, UE18, UF09, UG06, UK01, UL12, UM10, UM31, UP05, VA02, VC06, VD06, VE10    (b) RH14, RH21, RK18, RL15, RM01, RM22, RN24, RP01, TA19, TF05, TF27, TG19, TH20, TK24, TL01, TM12, TN09, TP03, UA20, UC15, UD22, UE04, UE18, UF02, UG13, UH11, UK15, UL06, UM10, VA02, VA30, VC27, VE03, VF01   LH130 PRODUCT CORRECTION lot codes or serial number range: TA19 through VD06, distribution date range: 08Apr2015 through 20Jan2017
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    No
  • 유통
    Worldwide distribution: US, Canada, Colombia, UK, Belgium, and Japan
  • 제품 설명
    TERUMO(R) Overpressure Safety Valve, REF: (a) LH130 (b) LH130J
하나 더 7 건 더

유사한 이름을 가진 의료기기 1건 유사한 이름을 가진 의료기기 13 건

데이터에 대해 더 자세히 알아보기 여기

  • 제조사 주소
    Terumo Cardiovascular Systems Corporation, 6200 Jackson Rd, Ann Arbor MI 48103-9586
  • 제조사 모회사 (2017)
  • Source
    USFDA
  • 제조사 주소
    Terumo Cardiovascular Systems Corporation, 6200 Jackson Rd, Ann Arbor MI 48103
  • 제조사 모회사 (2017)
  • Source
    USFDA
하나 더 8 건 더